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Variant (rsID / SNP)

rs1397548

ADGRL3

rs1397548 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRL3. Location: chromosome 4, position 62,845,490. The table records no clinical significance for this variant.

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Reference-table entries

ADGRL3Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
4:62845490
HGVS
NM_001387552.1,c.3015A>G,p.Pro1005Pro
Allele change
Synonymous_P937P

Associated conditions / phenotypes

Attention Deficit-Hyperactivity Disorder|Major Affective Disorder 8|Major Affective Disorder 9|Bipolar Disorder

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.